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GWAS Study

Non-coding genetic elements of lung cancer identified using whole genome sequencing in 13,722 Chinese.

Zhou D, Wu M, Tan Q et al.

40783572 PubMed ID
GWAS Study Type
13722 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ZD
Zhou D
WM
Wu M
TQ
Tan Q
SL
Sun L
TY
Tu Y
ZW
Zheng W
ZY
Zhu Y
YM
Yang M
HK
Hu K
HF
Hu F
XX
Xu X
ZH
Zhou H
LT
Luo T
YF
Yang F
LF
Li F
JX
Jin X
TH
Tu H
LW
Li W
WK
Wu K
WX
Wu X
Chapter II

Abstract

Summary of the research findings

A substantial portion of lung cancer-associated genetic elements in East Asian populations remains unidentified, underscoring the need for large-scale genome-wide studies, particularly on non-coding regulation. We conducted a whole genome sequencing (WGS)-based genome-wide scan in 13,722 Chinese individuals to identify regulatory elements associated with lung cancer. We verified common-variant-based loci by meta-analysis across the available East Asian studies. Integrating a genome-transcriptome reference panel of lung tissue in 297 Chinese, we bridged the variant-lung cancer associations, highlighting genes including TP63 and DCBLD1. Implementing the STAAR pipeline for rare variant aggregate analysis, we identified and replicated novel genes, including PARPBP, PLA2G4C, and RITA1 in the context of non-coding regulation. Adapting a deep learning-based approach, potential upstream regulators such as TP53, MYC, ZEB1, and NFKB1 were revealed for the lung cancer-associated genes. These findings offered crucial insights into the non-coding regulation for the etiology of lung cancer, providing additional potential targets for intervention.

1,104 Chinese ancestry cases, 9,635 Chinese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

13722
Total Participants
GWAS
Study Type
Yes
Replicated
1,487 Chinese ancestry cases, 1,496 Chinese ancestry controls
Replication Participants
East Asian
Ancestry
China
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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